Ubiquitination/ Proteasome
Ubiquitination/ Proteasome(泛素化/蛋白酶体)
Ubiquitination/ Proteasome 相关产品(1292)
- GC35601CaMKII-IN-1CAS: 1208123-85-6纯度: >99.50% / >98.00%
CaMKII-IN-1是一种强效且高度选择性的CaMKII抑制剂,IC 50 值为63nM。
- GC35820DDD107498 succinateCAS: 2444781-71-7纯度: >98.50%
DDD107498 (M-5717, DDD-498) is a P. falciparum translation elongation factor 2 inhibitor. DDD107498 exhibits a potent and novel spectrum of antimalarial activity against multiple life-cycle stages of the Plasmodium parasite.
- GC35832Dehydrocorydaline chlorideCAS: 10605-03-5纯度: >98.00%
An alkaloid with diverse biological activities
- GC35969eIF4A3-IN-1CAS: 2095486-67-0纯度: >99.50%
eIF4A3-IN-1 (compound 53a) 是一种选择性的真核起始因子 4A3 (eIF4A3) 抑制剂 (IC50=0.26 μM; Kd=0.043 μM),eIF4A3-IN-1 与 eIF4A3 的非 ATP 结合位点结合,并在 10 μM 和 3 μM 时明显抑制细胞无义介导的 RNA 衰变 (NMD), 可作为进一步研究 eIF4A3、外显子连接复合体 (EJC) 和 NMD 的探针。
- GC35998EpisilvestrolCAS: 697235-39-5纯度: >99.50%
Episilvestrol 是 silvestrol 的衍生物,从 Aglaia silvestris 中分到,能够抑制 eIF4A 靶作用的转录过程。
- GC36136Ginkgolide KCAS: 153355-70-5纯度: >99.50%
A terpene trilactone with diverse biological activities
- GC36163GlycycoumarinCAS: 94805-82-0纯度: >99.50%
Glycycoumarin 是一种甘草中主要的生物活性香豆素。Glycycoumarin 通过激活自噬,抑制内质网应激介导的 JNK 和 GSK-3 介导的线粒体途径,来抑制肝细胞脂性凋亡。Glycycoumarin 能直接靶向 T-LAK 细胞源蛋白激酶发挥抗肝癌活性 。
- GC36215Heparin Lithium saltCAS: 9045-22-1纯度: 不显示
Heparin Lithium salt 是一种抗凝剂,可与 抗凝血酶III (ATIII) 可逆地结合 (50-400 U/Kg)。
- GC36339IsorhapontigeninCAS: 32507-66-7纯度: >99.50%
Isorhapontigenin (ISOR), isolated from Belamcanda chinensis, is a derivative of stilbene. Isorhapontigenin possessed potent antioxidative activity. Isorhapontigenin suppresses interleukin-1β-induced inflammation and cartilage matrix damage in rat chondrocytes.
- GC36346Isosorbide mononitrateCAS: 16051-77-7纯度: >99.50%
A nitric oxide donor with cardioprotective activity
- GC36356Ixazomib citrateCAS: 1239908-20-3纯度: >99.50%
Ixazomib citrate (MLN9708, Ninlaro) is a prodrug of Ixazomib (MLN2238), which is a selective, orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic (β5) site with IC50 of 3.4 nM and Ki of 0.93 nM, respectively. Ixazomib (MLN2238) also inhibits caspase-like (β1) and trypsin-like (β2) proteolytic sites with IC50 of 31 nM and 3500 nM, respectively.
| 货号 | 产品名称 | CAS号 | 纯度 | 结构 |
|---|---|---|---|---|
| GC35555 | Britannin | 33627-28-0 | >99.50% | |
Britannin,分离于 Inula aucheriana,是倍半萜内酯。Britannin 通过激活由 ROS 调节的 AMPK 来诱导肝癌细胞凋亡和自噬。Britannin 具有抗增殖和抗炎活性。 | ||||
| GC35601 | CaMKII-IN-1 | 1208123-85-6 | >99.50% / >98.00% | |
CaMKII-IN-1是一种强效且高度选择性的CaMKII抑制剂,IC 50 值为63nM。 | ||||
| GC35613 | Carvedilol phosphate hemihydrate | 610309-89-2 | - | |
A β-adrenergic receptor antagonist | ||||
| GC35667 | CFTR corrector 1 | 2216712-66-0 | >99.50% | |
An F508del-CFTR corrector and potentiator | ||||
| GC35668 | CG-200745 | 936221-33-9 | - | |
CG-200745 (CG-200745) 是一种具有口服活性的强效 pan-HDAC 抑制剂,其异羟肟酸部分可与催化袋底部的锌结合。 CG-200745 抑制组蛋白 H3 和微管蛋白的去乙酰化。 CG-200745 诱导 p53 的积累,促进 p53 依赖性反式激活,并增强 MDM2 和 p21 (Waf1/Cip1) 蛋白的表达。 CG-200745 增强了吉西他滨耐药细胞对吉西他滨和 5-氟尿嘧啶 (5-FU;) 的敏感性。 CG-200745 诱导细胞凋亡并具有抗肿瘤作用。 | ||||
| GC35812 | Dasatinib hydrochloride | 854001-07-3 | >98.50% / >99.00% | |
An inhibitor of Abl and Src | ||||
| GC35820 | DDD107498 succinate | 2444781-71-7 | >98.50% | |
DDD107498 (M-5717, DDD-498) is a P. falciparum translation elongation factor 2 inhibitor. DDD107498 exhibits a potent and novel spectrum of antimalarial activity against multiple life-cycle stages of the Plasmodium parasite. | ||||
| GC35832 | Dehydrocorydaline chloride | 10605-03-5 | >98.00% | |
An alkaloid with diverse biological activities | ||||
| GC35969 | eIF4A3-IN-1 | 2095486-67-0 | >99.50% | |
eIF4A3-IN-1 (compound 53a) 是一种选择性的真核起始因子 4A3 (eIF4A3) 抑制剂 (IC50=0.26 μM; Kd=0.043 μM),eIF4A3-IN-1 与 eIF4A3 的非 ATP 结合位点结合,并在 10 μM 和 3 μM 时明显抑制细胞无义介导的 RNA 衰变 (NMD), 可作为进一步研究 eIF4A3、外显子连接复合体 (EJC) 和 NMD 的探针。 | ||||
| GC35982 | EN6 | 1808714-73-9 | >99.00% | |
An activator of autophagy | ||||
| GC35998 | Episilvestrol | 697235-39-5 | >99.50% | |
Episilvestrol 是 silvestrol 的衍生物,从 Aglaia silvestris 中分到,能够抑制 eIF4A 靶作用的转录过程。 | ||||
| GC36003 | Erlotinib mesylate | 248594-19-6 | - | |
An EGFR tyrosine kinase inhibitor | ||||
| GC36023 | FAAH inhibitor 1 | 326866-17-5 | - | |
FAAH inhibitor 1是一种选择性的、可逆的脂肪酸酰胺水解酶(FAAH)抑制剂,IC 50 值为18±8nM。 | ||||
| GC36061 | Fluvastatin D6 sodium | - | - | |
An internal standard for the quantification of fluvastatin | ||||
| GC36063 | FMK 9a | 1955550-51-2 | - | |
FMK 9a是autophagin-1的抑制剂,在FRET和LRA试验中测定的IC50值分别为80 和73 nM。 | ||||
| GC36130 | Gemcitabine elaidate | 210829-30-4 | >98.00% | |
A prodrug form of gemcitabine | ||||
| GC36136 | Ginkgolide K | 153355-70-5 | >99.50% | |
A terpene trilactone with diverse biological activities | ||||
| GC36149 | GLPG2451 | 2055015-61-5 | >99.50% | |
GLPG2451 是一种囊性纤维化跨膜电导调节器 (CFTR) 的增强剂,有效增强低温挽救的 F508del CFTR,EC50 为 11.1 nM。 | ||||
| GC36163 | Glycycoumarin | 94805-82-0 | >99.50% | |
Glycycoumarin 是一种甘草中主要的生物活性香豆素。Glycycoumarin 通过激活自噬,抑制内质网应激介导的 JNK 和 GSK-3 介导的线粒体途径,来抑制肝细胞脂性凋亡。Glycycoumarin 能直接靶向 T-LAK 细胞源蛋白激酶发挥抗肝癌活性 。 | ||||
| GC36215 | Heparin Lithium salt | 9045-22-1 | 不显示 | |
Heparin Lithium salt 是一种抗凝剂,可与 抗凝血酶III (ATIII) 可逆地结合 (50-400 U/Kg)。 | ||||
| GC36329 | Irinotecan hydrochloride | 100286-90-6 | >99.00% | |
A potent inhibitor of DNA topoisomerase I | ||||
| GC36339 | Isorhapontigenin | 32507-66-7 | >99.50% | |
Isorhapontigenin (ISOR), isolated from Belamcanda chinensis, is a derivative of stilbene. Isorhapontigenin possessed potent antioxidative activity. Isorhapontigenin suppresses interleukin-1β-induced inflammation and cartilage matrix damage in rat chondrocytes. | ||||
| GC36346 | Isosorbide mononitrate | 16051-77-7 | >99.50% | |
A nitric oxide donor with cardioprotective activity | ||||
| GC36356 | Ixazomib citrate | 1239908-20-3 | >99.50% | |
Ixazomib citrate (MLN9708, Ninlaro) is a prodrug of Ixazomib (MLN2238), which is a selective, orally bioavailable inhibitor of 20S proteasome that inhibits the chymotrypsin-like proteolytic (β5) site with IC50 of 3.4 nM and Ki of 0.93 nM, respectively. Ixazomib (MLN2238) also inhibits caspase-like (β1) and trypsin-like (β2) proteolytic sites with IC50 of 31 nM and 3500 nM, respectively. | ||||
